Substituted pteridinones, pyrimidines, pyrrolopyrimidines, and purines as p90 ribosomal S6 protein kinase-2 (RSK2) inhibitors: Pharmacophore modeling data-Reference-Cited by-同舟云学术

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Substituted pteridinones, pyrimidines, pyrrolopyrimidines, and purines as p90 ribosomal S6 protein kinase-2 (RSK2) inhibitors: Pharmacophore modeling data

Published:2021-10 Issue: Volume:38 Page:107433
ISSN:2352-3409
Container-title:Data in Brief
language:en
Short-container-title:Data in Brief

Author:

Warfield Becka M.^ORCID,Casalvieri Kimberly A.,Matheson Christopher J.^ORCID,Backos Donald S.^ORCID,Reigan Philip^ORCID

Publisher

Elsevier BV

Subject

Multidisciplinary

Reference12 articles.

1. Molecular docking of substituted pteridinones and pyrimidines to the ATP-binding site of the N-terminal domain of RSK2 and associated MM/GBSA and molecular field datasets;Casalvieri;Data Brief,2020

2. Substituted pteridinones as p90 ribosomal S6 protein kinase (RSK) inhibitors: A structure-activity study;Casalvieri;Bioorg. Med. Chem.,2020

3. N-Substituted pyrrolopyrimidines and purines as p90 ribosomal S6 protein kinase-2 (RSK2) inhibitors;Casalvieri;Bioorg. Med. Chem.,2021

4. Selective targeting of RSK isoforms in cancer;Casalvieri;Trends Cancer,2017

5. BI-D1870 is a specific inhibitor of the p90 RSK (ribosomal S6 kinase) isoforms in vitro and in vivo;Sapkota;Biochem. J.,2007

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